Laroche S - Search Results

1

The intellectual disability PAK3 R67C mutation impacts cognitive functions and adult hippocampal neurogenesis.

Castillon C, Gonzalez L, Domenichini F, Guyon S, Da Silva K, Durand C, Lestaevel P, Vaillend C, Laroche S, Barnier JV, Poirier R. Castillon C, et al. Among authors: laroche s. Hum Mol Genet. 2020 Jul 29;29(12):1950-1968. doi: 10.1093/hmg/ddz296. Hum Mol Genet. 2020. PMID: 31943058 Free article.

2

Reduced neuronal density in the CA1 anterodorsal hippocampus of the mdx mouse.

Miranda R, Laroche S, Vaillend C. Miranda R, et al. Among authors: laroche s. Neuromuscul Disord. 2016 Nov;26(11):775-781. doi: 10.1016/j.nmd.2016.08.006. Epub 2016 Aug 17. Neuromuscul Disord. 2016. PMID: 27614574

3

Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome.

Castillon C, Lunion S, Desvignes N, Hanauer A, Laroche S, Poirier R. Castillon C, et al. Among authors: laroche s. Neurobiol Dis. 2018 Jul;115:69-81. doi: 10.1016/j.nbd.2018.04.007. Epub 2018 Apr 6. Neurobiol Dis. 2018. PMID: 29627578

4

Thyroid Hormone Supplementation Restores Spatial Memory, Hippocampal Markers of Neuroinflammation, Plasticity-Related Signaling Molecules, and β-Amyloid Peptide Load in Hypothyroid Rats.

Chaalal A, Poirier R, Blum D, Laroche S, Enderlin V. Chaalal A, et al. Among authors: laroche s. Mol Neurobiol. 2019 Jan;56(1):722-735. doi: 10.1007/s12035-018-1111-z. Epub 2018 May 23. Mol Neurobiol. 2019. PMID: 29796989

5

Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin-deficient Dmd(mdx) mouse.

Vaillend C, Billard JM, Laroche S. Vaillend C, et al. Among authors: laroche s. Neurobiol Dis. 2004 Oct;17(1):10-20. doi: 10.1016/j.nbd.2004.05.004. Neurobiol Dis. 2004. PMID: 15350961

6

Genes, plasticity and mental retardation.

Vaillend C, Poirier R, Laroche S. Vaillend C, et al. Among authors: laroche s. Behav Brain Res. 2008 Sep 1;192(1):88-105. doi: 10.1016/j.bbr.2008.01.009. Epub 2008 Jan 31. Behav Brain Res. 2008. PMID: 18329113 Review.

7

Upregulation of brain utrophin does not rescue behavioral alterations in dystrophin-deficient mice.

Perronnet C, Chagneau C, Le Blanc P, Samson-Desvignes N, Mornet D, Laroche S, De La Porte S, Vaillend C. Perronnet C, et al. Among authors: laroche s. Hum Mol Genet. 2012 May 15;21(10):2263-76. doi: 10.1093/hmg/dds047. Epub 2012 Feb 15. Hum Mol Genet. 2012. PMID: 22343141

8

Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin-Lowry syndrome.

Morice E, Farley S, Poirier R, Dallerac G, Chagneau C, Pannetier S, Hanauer A, Davis S, Vaillend C, Laroche S. Morice E, et al. Among authors: laroche s. Neurobiol Dis. 2013 Oct;58:156-68. doi: 10.1016/j.nbd.2013.05.016. Epub 2013 Jun 3. Neurobiol Dis. 2013. PMID: 23742761

9

Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior.

Poirier R, Jacquot S, Vaillend C, Soutthiphong AA, Libbey M, Davis S, Laroche S, Hanauer A, Welzl H, Lipp HP, Wolfer DP. Poirier R, et al. Among authors: laroche s. Behav Genet. 2007 Jan;37(1):31-50. doi: 10.1007/s10519-006-9116-1. Epub 2006 Oct 11. Behav Genet. 2007. PMID: 17033934 Free article.

10

Altered presynaptic ultrastructure in excitatory hippocampal synapses of mice lacking dystrophins Dp427 or Dp71.

Miranda R, Nudel U, Laroche S, Vaillend C. Miranda R, et al. Among authors: laroche s. Neurobiol Dis. 2011 Jul;43(1):134-41. doi: 10.1016/j.nbd.2011.02.017. Epub 2011 Mar 22. Neurobiol Dis. 2011. PMID: 21397023

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